Author

Jill C. Hennessey

Observed names: J C Hennessey, Jill Hennessey

Institutions: Johns Hopkins University, Johns Hopkins Medicine

Observed institutions: Howard Hughes Medical Institute, Johns Hopkins University, Johns Hopkins Medicine, Foundation Fighting Blindness, Johns Hopkins Hospital, The University of Texas Health Science Center at Houston

OpenAlex ID: A5110170335

Rhodopsin mutations in autosomal dominant retinitis pigmentosa.

1991 · C H Sung, C M Davenport, et al. · Proceedings of the National Academy of Sciences · 464

Identification of novel rhodopsin mutations responsible for retinitis pigmentosa: implications for the structure and function of rhodopsin.

1993 · J P Macke, C M Davenport, et al. · Europe PMC (PubMed Central) · 141

Obesity in achondroplasia

1988 · Jacqueline T. Hecht, Opal Jean Hood, et al. · American Journal of Medical Genetics · 83

Familial tandem duplication of bands q31.1 to q32.3 on chromosome 4 with mild phenotypic effect

1997 · Barbara K. Goodman, George T. Capone, et al. · American Journal of Medical Genetics · 31

Increased sister chromatid exchange frequency at Xq27 site in affected fragile X males

1987 · Sharon L. Wenger, Jill C. Hennessey, et al. · American Journal of Medical Genetics · 26

Rhodopsin mutation proline347-to-alanine in a family with autosomal dominant retinitis pigmentosa indicates an important role for proline at position 347

1995 · Jennifer P. Macke, Jill C. Hennessey, et al. · Human Molecular Genetics · 21

Works count: 6

Citation count: 766

H-index: 6

I10-index: 6